ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.503-8C>G

dbSNP: rs606231313
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Evolutionary and Medical Genetics Laboratory, Centre for Cellular and Molecular Biology RCV000148987 SCV000154236 unknown Familial cardiomyopathy no assertion criteria provided not provided Converted during submission to Uncertain significance.

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